Cra Ii, Oncology

IQVIA UK

Manchester, United Kingdom
Independent on-site monitoring
Managing multiple clinical trial protocols
Knowledge of gcp and ich guidelines
Join IQVIA on our mission to accelerate innovation for a healthier world

Job Summary

  • Join IQVIA on our mission to accelerate innovation for a healthier world.
  • We are recognised as a 2026 Glassdoor Best Place to Work in the UK.
  • Apply today and forge a career with greater purpose, make an impact, and never stop learning!

Matching Summary

Join IQVIA on our mission to accelerate innovation for a healthier world.

Skills & Requirements

Must-have

  • independent on-site monitoring
  • managing multiple clinical trial protocols
  • knowledge of GCP and ICH guidelines

Nice-to-have

  • flexibility to travel to sites
  • strong communication skills
  • team collaboration

Key Requirements

  • life science degree or equivalent experience
  • experience in clinical trials

Work Rights

Not specified

Tailored Resume

Cover Letter